About Phenylketonuria II

Hyperphenylalaninemia, Bh4-Deficient, C, also known as dihydropteridine reductase deficiency, is related to hyperphenylalaninemia, bh4-deficient, a and phenylketonuria, and has symptoms including seizures and tremor. An important gene associated with Hyperphenylalaninemia, Bh4-Deficient, C is QDPR (Quinoid Dihydropteridine Reductase). Affiliated tissues include heart, skin and brain, and related phenotypes are intellectual disability and dysphagia

Major Symptoms of Phenylketonuria II

Phenylketonuria II is a rare genetic disorder that primarily affects children. It is characterized by the inability to break down certain proteins, leading to a buildup of protein waste in the body. Symptoms include progressive muscle weakness, bone and joint pain, and intellectual disabilities. Additionally , individuals with Phenylketonuria II may experience skin rashes and itching.

Suitable Lifestyle for People with Phenylketonuria II

The suitable lifestyle for people with Phenylketonuria II includes the following points:

1. Avoid eating foods that may cause symptoms: Patients need to avoid eating foods that may cause symptoms, such as tyrosine, phenylalanine, tryptophan, etc. .

2. Maintain a regular work and rest schedule: Maintaining a regular work and rest schedule and ensuring adequate sleep will help with recovery from illness.

3. Carry out appropriate exercise: Proper exercise can help improve the body's immunity and reduce symptoms of the disease.

4. Maintain a good attitude: Maintaining a good attitude and avoiding excessive anxiety and worry can help with recovery from the disease.

5. Follow the doctor's advice: Patients need to follow the doctor's advice, take medicine on time, and check their condition regularly to help recover from the disease.

6. Maintain good hygiene habits: Patients need to maintain good hygiene habits, wash hands frequently, and pay attention to personal hygiene to help reduce symptoms.

Other Diseases

Phenylketonuria Phenylketonuria in Children

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